76335-79-0

Upstream product

• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 

Downstream Products

• 13330-65-9 2,4-dimethoxyphenol 
• 100-51-6 benzyl alcohol 
• 132114-78-4 (2,4-Dimethoxy-phenoxy)-trimethyl-silane 
• 88775-56-8 2-(5-benzyloxy-2,4-dimethoxyphenyl)-4-(3,4-dimethoxyphenyl)-4-oxobutyramide 
• 88775-55-7 2-(5-benzyloxy-2,4-dimethoxyphenyl)-4-(3,4,-dimethoxyphenyl)-4-oxobutyronitrile 
• 88775-53-5 5-benzyloxy-2,4,3',4'-tetramethoxychalcone 
• 76335-80-3 5-benzyloxy-2,4-dimethoxybenzaldehyde 

Relevant academic research and scientific papers

29Si and 13C NMR Spectra of 4-Substituted 2-Methoxytrimethylsiloxybenzenes. Factors Determining the Chemical Shifts in Models of Lignin Constituents

29Si and 13C NMR chemical shifts are reported for a series of twenty 4-substituted 2-methoxytrimethylsiloxybenzenes; the set of substituents incorporates a basic set of ten substituents differing in their relative polar and resonance effects and ten other

Studies on the chemical constituents of rutaceous plants. XLIX. Development of a versatile method for the synthesis of antitumor-active benzo[c]phenanthridine alkaloids. (1). Preparation of various 2,4-bisaryl-4-oxobutyronitriles and 2,4-bisaryl-4-oxobutyramides

For the sake of establishment of a versatile synthetic method for benzo[c]phenanthridine alkaloids, improvement of the Robinson synthetic method was examined. Thirteen chalcones (7a-m) were prepared by condensation of two acetophenone derivatives (15 and 16) with eleven benzaldehyde derivatives (19a-k) as fundamental starting materials. Hydrocyanation of these chalcones (7a-1) except one (7m) gave the corresponding 2,4-bisaryl-4-oxobutyronitriles (8a-1). Eleven 2,4-bisaryl-4-oxobutyramides (9a-k) were also prepared.